Canonical Allele Identifier: CA2697551040

Gene: ZEB2

Linked Data

• ClinVar Variation Id: 2707202
• ClinVar RCV Id: RCV003503640

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144399281dup , CM000664.2:g.144399281dup	GRCh38
NC_000002.11:g.145156848dup , CM000664.1:g.145156848dup	GRCh37
NC_000002.10:g.144873318dup	NCBI36
NG_016431.1:g.126112dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*1756dup	ENSP00000508434.1:n.*1756dup
ENST00000440875.6:c.1130dup	ENSP00000475553.3:p.Leu377PhefsTer7
ENST00000627532.3:c.1907dup MANE Select	ENSP00000487174.1:p.Leu636PhefsTer7
ENST00000636026.2:c.1907dup	ENSP00000490776.1:p.Leu636PhefsTer7
ENST00000636179.1:n.1876dup
ENST00000636413.1:c.1571dup	ENSP00000490508.1:p.Leu524PhefsTer7
ENST00000636471.1:c.1982dup	ENSP00000490317.1:p.Leu661PhefsTer7
ENST00000636732.2:c.*1624dup	ENSP00000490175.1:n.*1624dup
ENST00000636820.1:n.2007dup
ENST00000637045.1:c.1571dup	ENSP00000490141.1:p.Leu524PhefsTer7
ENST00000637304.1:c.1571dup	ENSP00000490872.1:p.Leu524PhefsTer7
ENST00000638007.1:c.1571dup	ENSP00000490723.1:p.Leu524PhefsTer7
ENST00000638087.1:c.1571dup	ENSP00000490673.1:p.Leu524PhefsTer7
ENST00000638128.1:c.1130dup	ENSP00000490934.1:p.Leu377PhefsTer7
ENST00000675069.1:c.-133-430dup	ENSP00000502467.1:n.-133-430dup
ENST00000675145.1:n.2455dup
ENST00000303660.8:c.1904dup	ENSP00000302501.4:p.Leu635PhefsTer7
ENST00000409487.7:c.1907dup	ENSP00000386854.2:p.Leu636PhefsTer7
ENST00000419938.5:c.655+1919dup	ENSP00000394777.2:n.655+1919dup
ENST00000427902.5:c.1994dup	ENSP00000395496.2:p.Leu665PhefsTer7
ENST00000440875.5:c.1167+257dup	ENSP00000475553.2:n.1167+257dup
ENST00000539609.7:c.1835dup	ENSP00000443792.2:p.Leu612PhefsTer7
ENST00000558170.6:c.1907dup	ENSP00000454157.1:p.Leu636PhefsTer7
ENST00000627532.2:c.1907dup	ENSP00000487174.1:p.Leu636PhefsTer7
NM_001171653.1:c.1835dup	NP_001165124.1:p.Leu612PhefsTer7
NM_014795.3:c.1907dup	NP_055610.1:p.Leu636PhefsTer7
XM_006712881.2:c.1907dup	XP_006712944.1:p.Leu636PhefsTer7
XM_006712882.2:c.1907dup	XP_006712945.1:p.Leu636PhefsTer7
XM_011512231.1:c.1898dup	XP_011510533.1:p.Leu633PhefsTer7
XM_011512232.1:c.1886dup	XP_011510534.1:p.Leu629PhefsTer7
NM_014795.4:c.1907dup MANE Select	NP_055610.1:p.Leu636PhefsTer7
NM_001171653.2:c.1835dup	NP_001165124.1:p.Leu612PhefsTer7